High-throughput SNP genotyping

被引:47
|
作者
Jenkins, S [1 ]
Gibson, N [1 ]
机构
[1] AstraZeneca, R&D Genet, Macclesfield SK10 4TG, Cheshire, England
来源
COMPARATIVE AND FUNCTIONAL GENOMICS | 2002年 / 3卷 / 01期
关键词
SNP; genotyping technology; genetic variation; sequence detection; SNP detection; allelic discrimination; high-throughput;
D O I
10.1002/cfg.130
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Whole genome approaches using single nucleotide polymorphism (SNP) markers have the potential to transform complex disease genetics and expedite pharmacogenetics research. This has led to a requirement for high-throughput SNP genotyping platforms. Development of a successful high-throughput genotyping platform depends on coupling reliable assay chemistry with an appropriate detection system to maximise efficiency with respect to accuracy, speed and cost. Current technology platforms are able to deliver throughputs in excess of 100 000 genotypes per day, with an accuracy of >99%, at a cost of 20-30 cents per genotype. In order to meet the demands of the coming years, however, genotyping platforms need to deliver throughputs in the order of one million genotypes per day at a cost of only a few cents per genotype. In addition, DNA template requirements must be minimised such that hundreds of thousands of SNPs can be interrogated using a relatively small amount of genomic DNA. As such, it is predicted that the next generation of high-throughput genotyping platforms will exploit large-scale multiplex reactions and solid phase assay detection systems. Copyright (C) 2001 John Wiley Sons, Ltd.
引用
收藏
页码:57 / 66
页数:10
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